6-Ethyl-3- metabolic fate

The metabolic fate of chlordan was studied in rabbits by analysis of the relative chlorine content of chlordan added to normal rabbit s urine and of the chlorine content of the urinary excretory product. The method of analysis was similar to the one previously used (, 4) In addition, hydrolysis of chlordan and of the urinary excretory products was carried out by adding solid sodium hydroxide to saturation to a 10-ml. solution of these substances in hot absolute ethyl alcohol. The mixture was refluxed for 3 hours in a round-bottomed flask immersed in boiling water and the amount of inorganic chlorine determined. Hydrolysis was similarly carried out with solutions of the respective substances in aqueous sodium hydroxide. 

The 3,4-dihydrodiol is a major component of the free dihydrodiols formed in mouse skin maintained in short-term culture (28). The optical purities of these dihydrodiols were determined by a CSP-HPLC method (43). The metabolic fates of the enantiomeric DMBA 3,4-dihydrodiols are not yet known. Studies in our laboratory indicate that the products formed in liver microsomal metabolism of DMBA 3,4-dihydrodiol bind extensively to the components of liver microsomes and the expected 1,2,3,4-tetrols of DMBA were not detected in the acetone/ethyl acetate extract of the incubation mixture (unpublished results). It is known that these products bind extensively to DNA... 

Alkylthiotriazines. In our laboratory we have studied the metabolic fate of 2-(4-ethylamino-6-methylthio- -triazin-2-ylamino)-2-methylpropionitrile (cyanatryn, 1, Fig. 1). This compound is a member of a class of herbicidal -triazines which also includes ametryne, prometryne and terbutryne. We were interested to note ( ) that two of the major metabolites of cyanatryn were the mercapturic acids 2-[A-ethylamino-6-(N-acetylcysteinyl)- -triazin-2-ylamino]-2-methylpropionitrTle (2.1) and its N-de-ethyl derivative (2.2) (Fig. 2). This pathway had not hitherto been reported for this class of compound. 

Investigation of the metabolic fate of compounds 64b and 71b led to the following results After peroral administration of 71b in rats, about 90% of the ingested silicon could be detected in urine within 4 days. In the ethyl ether extract of the urine, no unchanged 71b could be found. In the ethyl acetate extract the dealkylation product 85 was detected (29% of ingested sila-carbamate 71b) ... 

The occlusive study for C-phenyl-2-ethyl-6-methyl aniline hydrochloride (MEA) was done to observe the metabolic fate and urine oietabolices. Defining a major urinary component would serve as an appropriate measure of exposure to The major... 

Fourteen members of this group of flavouring substances, ethane-1,1 -dithiol (No. 1660), 4-mercapto-2-pentanone (No. 1670), diisopentyl thiomalate (No. 1672), cis- and frans-mercapto-p-menthan-3-one (No. 1673), 2,4,6-trithiaheptane (No. 1684), ( )-2,8-epithio-c/s-p-menthane (No. 1685), mixture of 3,6-diethyl-1,2,4,5-tetrathiane and 3,5-diethyl-1,2,4-trithiolane (No. 1687), ( )-3-(methylthio)heptanal (No. 1692), ethyl methyl disulfide (No. 1693), ethyl propyl trisulfide (No. 1695), methyl isopentyl disulfide (No. 1696), butyl ethyl disulfide (No. 1698), allyl propyl disulfide (No. 1700) and bis(1-mercaptopropyl)sulfide (No. 1709), have assay values of <95%. Information on the safety of the secondary components of these 14 compounds is summarized in Annex 5 (Summary of the safety evaluation of secondary components for flavouring agents with minimum assay values of less than 95%). The secondary component of diisopentyl thiomalate, diisopentyl thiotartronate, is expected to share the same metabolic fate as the primary substance. The secondary components of frans-mercapto-p-menthan-3-one, piperitone (No. 435) and a-terpineol (No. 366), are expected to undergo rapid absorption, distribution, metabolism and excretion and were evaluated at previous... 

The concentration of CLA in plasma lipids is determined by bioavailability from the gut, and subsequent partitioning between p-oxidation, incorporation into tissue lipids, secretion from the gut and liver, and turnover within the plasma compartment. There is only limited information available about the metabolic fate of CLA in humans. Using deuterated fatty acid ethyl esters, Emken et al. (2002) showed that the bioavailability of cis-9,tram- CLA and trans- 0,cis- 2 CLA after a bolus was lower than that of oleic acid. However, since the fatty acids were not ingested as TAG any effect of the conjugated double bonds... 

Nozawa, T., Minami, H., Sugiura, S., Tsuji, A. and Tamai, I. (2005) Role of organic anion transporter OATP1B1 (OATP-C) in hepatic uptake of irinotecan and its active metabolite, 7-ethyl-10-hydroxycamptothecin in vitro evidence and effect of single nucleotide polymorphisms. Drug Metabolism and Disposition The Biological Fate of Chemicals, 33, 434-439. 

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